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Synthesis of Ferrocene‐Modified Carbon Nitride Photocatalysts by Surface Amidation Reaction for Phenol Synthesis
Author(s) -
Ye Xiangju,
Zheng Yun,
Wang Xinchen
Publication year - 2014
Publication title -
chinese journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.28
H-Index - 41
eISSN - 1614-7065
pISSN - 1001-604X
DOI - 10.1002/cjoc.201400229
Subject(s) - chemistry , photocatalysis , graphitic carbon nitride , benzene , phenol , diffuse reflectance infrared fourier transform , carbon nitride , x ray photoelectron spectroscopy , photochemistry , catalysis , ferrocene , electron paramagnetic resonance , visible spectrum , electrochemistry , organic chemistry , chemical engineering , electrode , physics , optoelectronics , nuclear magnetic resonance , engineering
A polymeric Fc‐CO‐NH‐C 3 N 4 (Fc‐CN) material was synthesized by amidation reaction of ferrocenecarboxylic acid (Fc‐COOH) with NH 2 groups on the surface of mesoporous graphitic carbon nitride (MCN). The properties of the as‐synthesized samples were characterized by X‐ray diffraction, Fourier transform infrared spectroscopy, UV‐Vis diffuse reflectance spectra, N 2 adsorption‐desorption isotherm, photoluminescence spectroscopy, transmission electron microscopy, electron paramagnetic resonance, (photo)electrochemical measurement and X‐ray photoelectron spectroscopy. The resultant catalysts were investigated as heterogeneous catalysts for the selective oxidation of benzene to phenol using H 2 O 2 as a green oxidant under visible light irradiation. The results reveal that Fc‐modified samples can not only extend the visible light absorption, but also accelerate the bulk‐to‐surface charge transfer and separation via surface dyadic structures, both of which are favorable for phenol production from benzene photocatalytic hydroxylation with H 2 O 2 . Under the optimal conditions, up to 16.9 % phenol yield (based on benzene) is obtained by Fc‐CN /1.5 ‐5 sample, and the corresponding Fe content is about 0.64 wt%. Furthermore, after the second run, no significant decrease of the activity (in term of TOF) and the selectivity is found in Fc‐CN /1.0 ‐5 sample. Combined with the experimental results and Fenton‐chemistry, a possible photocatalytic reaction mechanism on the hydroxylation of benzene to phenol at neutral medium with visible light is proposed.